欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/3900/001
药品名称Rivaroxaban Sandoz 10 mg, filmomhulde tabletten
活性成分
    • RIVAROXABAN 10.0 mg
剂型Film-coated tablet
上市许可持有人Sandoz B.V. Hospitaaldreef 29 1315 RC Almere The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Rivaroxaban Sandoz 10 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Austria (AT)
    • Greece (GR)
    • Poland (PL)
      Runaplax
    • Latvia (LV)
      Runaplax 10 mg apvalkotās tabletes
    • Lithuania (LT)
      Runaplax 10 mg plėvele dengtos tabletės
    • Estonia (EE)
      RUNAPLAX
    • Bulgaria (BG)
      Runaplax
    • Czechia (CZ)
      Rivaroxaban Sandoz 10 mg
    • Romania (RO)
    • Slovenia (SI)
    • Croatia (HR)
      Runaplax 10 mg filmom obložene tablete
许可日期2017/09/01
最近更新日期2024/08/22
药物ATC编码
    • B01AF01 rivaroxaban
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Multiple (Copy) Application
  • TypeLevel3：Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
附件文件下载
市场状态Positive
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